102060-67-3

Upstream product

• 133493-38-6 1-phenyl-2-(4-phenyl-1⁽³⁾H-imidazol-2-ylmercapto)-ethanone 
• 2010-06-2 2-Amino-4-phenylthiazole 
• 70-11-1 α-bromoacetophenone 
• 25752-18-5 6-phenylimidazo[2,1-b]-1,3,4-thiadiazole 
• 536-74-3 phenylacetylene 

Downstream Products

• 93329-14-7 5-nitroso-3,6-diphenyl-imidazo[2,1-b]thiazole 
• 1268167-82-3 C₁₇H₁₁IN₂S 
• 1268167-79-8 C₁₈H₁₁F₃N₂S 
• 92082-02-5 2,3,6-triphenylimidazo[2,1-b]thiazole 
• 1333080-06-0 C₂₃H₁₅FN₂S 
• 1333080-03-7 C₂₄H₁₈N₂S 
• 1333080-08-2 C₂₇H₁₈N₂S 
• 1333080-04-8 C₂₄H₁₈N₂OS 
• 1333080-07-1 C₂₄H₁₅F₃N₂S 
• 1333080-05-9 C₂₅H₂₀N₂S 

Relevant academic research and scientific papers

Approach for 2-(arylthio)imidazoles and imidazo[2,1-b]thiazoles from imidazo[2,1-b][1,3,4]thiadiazoles by ring-opening and -reconstruction

A highly efficient one-pot synthesis of imidazo[2,1-b]thiazole derivatives has been developed and proceeds via a ring-opening and ring-closing reconstruction of imidazo[2,1-b][1,3,4]thiadiazoles with phenylacetylene in the presence of potassium tert-butox

Ligand-free copper-catalyzed regioselective C-2 arylation of imidazo[2,1-b]thiazoles

An effective, regioselective C-2 arylation of imidazo[2,1-b]thiazoles catalyzed by Cu(I) has been developed. This arylation proceeded smoothly without promotion of the ligands, and various functional (22 samples) groups were well tolerated. Preliminary mechanistic studies of this arylation are also reported.

Synthesis of Styryl Dyes: Part I - Condensation of 2-Substituted N-Phenacylthiazolium Bromides with p-N,N-dimethylaminobenzaldehyde

Styryl dyes (2) have been synthesized by condensing 2-amino-3-phenacylthiazolium bromide (1) with p-N,N-dimethylaminobenzaldehyde (DAB).The unusual UV absorption data of 2 are due to in situ cyclisation leading to the formation of imidazo2,1-b)thiazole system.